Efficient synthesis of azetidine throughN-trityl- orN-dimethoxytritylazetidines starting from 3-amino-l-propanol or 3-halopropylamine hydrohalides
Author:
Publisher
Wiley
Subject
Organic Chemistry
Reference64 articles.
1. Synthesis of Azetidine from 1-Substituted Azetidin-3-ols
2. Pyrroloisoquinoline antidepressants. 2. In-depth exploration of structure-activity relationships
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1. Ring opening of azetidine cycle: First examples of 1-azetidinepropanamine molecules as a template in hybrid organic-inorganic compounds;Journal of Molecular Structure;2018-01
2. Tritylamine (triphenylmethylamine) in organic synthesis; III. The synthesis of 1-aminoalkylphosphonic acids in the reaction of N-(triphenylmethyl)alkanimines with phosphorus trichloride in acetic acid or with phosphonic acid in acetic anhydride.;Arkivoc;2010-12-05
3. ChemInform Abstract: Efficient Synthesis of Azetidine Through N-Trityl- or N- Dimethoxytritylazetidines Starting from 3-Amino-1-propanol or 3- Halopropylamine Hydrohalides.;ChemInform;2010-08-19
4. Regioselective synthesis of azetidines or pyrrolidines by selenium-induced cyclization of secondary homoallylic amines;Tetrahedron Letters;2010-08
5. Molecular and crystalline structures of three (S)-4-alkoxycarbonyl-2-azetidinones containing long alkyl side chains from synchrotron X-ray powder diffraction data;Acta Crystallographica Section B Structural Science;2009-11-16
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